Blog Posts
Explore timely perspectives from WCG’s clinical trial operations and scientific leaders.
Clinical Trial Safety
Submitting Deviations from a Sponsor’s Adverse Event Reporting Requirements to the IRB
Blog Posts
COVID-19
Informed Consent: An IRB Perspective on Navigating the New Normal
Blog Posts
Clinical Endpoints
New Normal or Not, Safety Reporting Matters
Blog Posts
Series: Ask the IRB & IBC Experts
What documentation is needed to prove a parent’s legal authority to consent for a child’s participation in research?
Blog Posts
Clinical Endpoints
From the Innovation Lab: Practical Challenges and Trade-offs with Wrist-Worn Devices for Clinical Trials
Blog Posts
COVID-19
There is Value to Patients When Independent Sites Offer Clinical Trials
Blog Posts
COVID-19
Through the Patient Lens: The Patient’s New Normal in Society’s New Abnormal
Blog Posts
Hybrid & Decentralized Trials
What are the regulations for training home health individuals who are working remotely to collect study data?
Blog Posts
Series: Ask the IRB & IBC Experts
Should Consent Form updates be aligned with Investigator Brochure updates, or wait for next Protocol amendment?
Blog Posts
COVID-19